HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243571Generated: October 30, 2026
Trifluoroacetic acid → HCID 11663885, compound
https://huagongshe.com/reaction/2243571
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 58608133 | HCID 58608133 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11663885 | HCID 11663885 | — |
Reaction Steps
A solution of 4-(2-{2-[4-(2-diisopropylamino-ethoxy)-phenyl]-3-phenyl-furo[2,3-b]pyridin-4-ylamino}-ethyl)-piperazine-1-carboxylic acid tert-butyl ester 10a (0.075 g, 0.117 mmol) in dichloromethane (2.0 mL) was cooled to 0° C. Trifluoroacetic acid (1.0 mL) was added and the solution stirred under a nitrogen atmosphere at 0° C. and was allowed to warm to room temperature over 2 h. The reaction mixture was concentrated and the residue was partitioned between dichloromethane and saturated aqueous sodium bicarbonate solution. The organic phase was separated and washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated to afford {2-[4-(2-diisopropylamino-ethoxy)-phenyl]-3-phenyl-furo[2,3-b]pyridin-4-yl}-(2-piperazin-1-yl-ethyl)-amine 10b as an off-white solid. MS (MH+) 542.3; Calculated 541 for C33H43N5O2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674907B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-79c72c6437794c7088557a73ffaa99c5 |
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| Source note | uspto-grants-2010_03 |
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